Clinical relevance of short-chain acyl-CoA dehydrogenase (SCAD) deficiency: Exploring the role of new variants including the first SCAD-disease-causing allele carrying a synonymous mutation
Open Access
- 1 June 2016
- journal article
- Published by Elsevier BV in BBA Clinical
- Vol. 5, 114-119
- https://doi.org/10.1016/j.bbacli.2016.03.004
Abstract
No abstract availableKeywords
Funding Information
- AMMeC (Associazione Malattie Metaboliche e Congenite, Italia) (1/14-15)
- Fondazione Meyer ONLUS, Firenze
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